Measuring the impact of soybean health on soybean diseases.
Management practices to alter the soil community structure will be implemented in replicated research plots at the Southeast Research and Extension Center fields in Parsons, KS. Treatments will include two treatments that are likely to increase disease (soybeans and corn stubble, both hosts of disease organisms), three treatments that are likely to decrease disease (brassica cover crop, animal manure, and solarization), and a fallow control. We will also be testing different soybean cultivars from MG 3.5 – 4.9 with different susceptibilities to disease. The soybean variety test plots at Ottawa will also be sampled to measure differences in plant and soil disease for MG 3.5 and MG 4.9. Additional test sites include sixteen fields at production farmers in eastern Kansas.
Testing will include several cultivars of soybeans with noted sensitivity to charcoal rot and sudden death (disease susceptibility: 9 = excellent; 1 = poor.):
Cultivar Maturity Group SCN Resistance Source Phytophthora resistance gene Sudden Death Syndrome Susceptibility Charcoal Rot Susceptibility
P35T15E 3.5 P188788 1k 5 4
P38454E 3.8 P188788 1a 7 8
P42T31E 4.2 P188788 - 5 4
P45T88E 4.5 P188788 ^1k 6 8
P49T74E 4.9 P188788 ^1c, ^1k 5 4
Phytophthora resistance gene: 1a: Provides resistance to races 1, 2, 10, 11, 13-18, 24, 26, 27, 31, 32 & 36. 1c: Provides resistance to races 1-3, 6-11, 13, 15, 17, 21, 23, 24, 26, 28-30, 32, 34, 36. 1k: Provides resistance to races 1-11, 13-15, 17, 18, 21-24, 26, 36, 37. (-) no specific gene for resistance
Soils will be sampled at three times during the season to determine: soil nutrients, soil community structure, and pathogen populations. Soils will be sampled prior to implementation of treatments (early March), mid-season (late June-July) and after harvesting soybeans (Sept. – Oct.). Final soybean yield will be collected.
The Soil Management Assessment Framework has identified five factors that are indicative of soil microbial activity. SMAF has been adopted by the NRCS as an indicator of soil health. These factors include: organic carbon, nitrogen, active carbon, wet aggregate stability, and soil respiration. These factors give an indication of the activity of the soil microbiome, though they do not measure the microbes directly. Total microbial biomass and the ratio of fungi to bacteria have also been shown to be related to disease suppression in soils.
Soil nutrients are important for growth of both microbes and plants. These will be measured at the K-State Soil Testing Lab, and include: pH, total organic matter, N, P, K, total organic carbon, total N, NO3-N, NH4-N, along with key micronutrients S, Ca, Mg, and Na. Wet aggregate stability will be measured using the soil volumetric aggregate stability test (VAST) from Solvita. Soil respiration will be measured with the CO2 Burst Test by Solvita. In addition, we will quantitate the disease presence of Macrophomina in soil and plants at three time points during the growing season (prior to planting, mid-season, and at harvest) by measuring CFUs.
This past year, we tested total soil microbial biomass and fungal:bacterial ratio with the MicroBIOMETER system. Unfortunately, results were not clear, and the test was disappointing. An examination of other potential disease organisms would be possible through PCR tests with disease-specific primers. This test would give a qualitative measure of disease presence and, in addition to Macrophomina, and allow detection of Fusarium, Phytophthora, Phomopsis, and Pythium. This analysis is expensive and beyond the scope of this proposal. We have submitted a funding request to SARE to pursue this research. We will continue to explore methods and funding sources to measure and quantitate total soil microbial biomass and fungal:bacterial ratios, and detection of disease organisms as an indication of “soil health”.
M. phaseolina populations will be determined by counting the number of colony-forming units (CFUs). Charcoal rot disease severity will be measured by randomly selecting ten plants per plot at the R7-R8 growth stage for root and stem severity ratings. The plants will be scored by splitting the stem and taproot of each plant and rating the degree of gray discoloration and microsclerotia in the vascular and cortical tissues on a scale of 1-5. M. phaseolina root populations will be estimated by grinding the split roots after the severity evaluation. The ground plant tissue and soil samples will be plated on microbiological media and incubated. CFUs of M. phaseolina will be counted and transformed to CFUs per gram of root tissue or gram of soil.